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Resistance to thyrotropin.

机译:对促甲状腺激素的抵抗。

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摘要

Resistance to TSH is a syndrome of reduced sensitivity to a biologically active TSH molecule. Subjects have elevated TSH levels but no goiter. However, thyroid hormone concentration may vary from normal to very high, depending on the severity of the resistance. Individuals with very high TSH, low T4 and hypoplastic thyroid glands can be mistakenly diagnosed as having primary hypothyroidism due to a defective development of the thyroid gland. Those with normal or slightly decreased T4 can be misdiagnosed as having central hypothyroidism especially if their serum TSH concentration is only slightly elevated. Mutations in the TSH receptor (TSHr) gene have been reported in 16 families with homozygous or compound heterozygous inheritance. The mutant TSHrs show reduced or no function due to either altered ligand binding or defect in membrane targeting. Some individuals, heretozygous for a TSHr gene mutation can present mild resistance to TSH manifesting as euthyroidism with slight hyperthyrotropinemia. A larger proportion of families express the phenotype of resistance to TSH in the absence of a TSHr defect. In many the inheritance is dominant and the genetic cause has not been yet determined.
机译:对 TSH 的耐药性是一种对生物活性 TSH 分子敏感性降低的综合征。受试者的 TSH 水平升高,但没有甲状腺肿。然而,甲状腺激素浓度可能从正常到非常高不等,具体取决于抵抗力的严重程度。由于甲状腺发育缺陷,TSH 非常高、T4 低和甲状腺发育不良的个体可能会被错误地诊断为原发性甲状腺功能减退症。T4 正常或略有降低的患者可能被误诊为中枢性甲状腺功能减退症,尤其是当他们的血清 TSH 浓度仅略有升高时。据报道,TSH 受体 (TSHr) 基因突变在 16 个具有纯合或复合杂合遗传的家族中。突变型TSHr由于配体结合改变或膜靶向缺陷而显示功能降低或无功能。一些个体,TSHr 基因突变的异端合子,可以表现出对 TSH 的轻度抵抗,表现为甲状腺功能正常伴轻度高促甲状腺激素血症。在没有TSHr缺陷的情况下,更大比例的家族表达了对TSH的抗性表型。在许多病例中,遗传是显性的,遗传原因尚未确定。

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